MR Spectroscopy as a Diagnostic and Outcome Measure in Pain and SCI
CompletedNCT00561782
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The goal of this study is to compare the changes that occur in sensation and chemical properties of the brain following SCI between individuals that experience chronic pain and those that do not, and between those with SCI and the able-bodied.
Study details
- Official title
- MR Spectroscopy (MRS) as a Diagnostic and Outcome Measure in Pain and SCI
- Conditions
- Spinal Cord Injury
- Hyperalgesia, Secondary
- Hyperalgesic Sensations
- Sponsor
- US Department of Veterans Affairs
- Collaborators
- University of Miami
- Organization
- VA Office of Research and Development
- Start date
- 2007-10
- Primary completion
- 2010-11
- Sex
- All
- Age range
- from 18 Years to 70 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. SCI and neuropathic pain: * fluent in English * incomplete or complete traumatic SCI * the injury must have occurred at least 2 years prior to entering the study * the injury level must be above L1 and the subjects must have evidence of preserved distal cord functions (lower extremity reflexes and bulbocavernosus or anal wink reflexes) * must have experienced chronic neuropathic pain at or below the level of injury for a minimum of six months * must have moderately severe or greater neuropathic pain * must be able to attend three sessions ranging from 2 to 6 hours over a period of 4 to 5 weeks 2. SCI and no neuropathic pain: \- same as a., but participants in this group must NOT have unremitting moderate-severe pain and there will only be two sessions ranging from 2 to 6 hours over a period of 1 to 2 weeks 3. Able-bodied control subjects: * fluent in English * no history of chronic pain conditions * no substantial brain or body injury * must be able to attend two sessions ranging from 2 to 6 hours over a period of 1 to 2 weeks Exclusion Criteria: * current pregnancy or women who are contemplating pregnancy * recent (one-year) history of alcohol or drug abuse * known intra-cerebral pathology or epilepsy * MRI findings indicative of intra-cerebral pathology * significant post-traumatic encephalopathy from head trauma sustained at SCI or cognitive impairment indicative of traumatic brain injury * current diagnosis of DSM-IV Axis I disorder * inability to meet the MRI screening requirements (including, but not limited to, the presence of a pacemaker or other electronic devices, prosthesis, artificial limb or joint, shunt, some metal rods, some tattoos, or moderate to severe claustrophobia or anxiety)
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00561782